NCT05886946

Brief Summary

This study aims to determine the value of ABG measurments in patients with blunt chest trauma and its role in prognosis of different outcomes and the results would aid the emergency physicians to speed up the management and reduce the cost of diagnosis

Trial Health

35
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
150

participants targeted

Target at P50-P75 for all trials

Timeline
Completed

Started Jul 2023

Status
unknown

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

May 24, 2023

Completed
9 days until next milestone

First Posted

Study publicly available on registry

June 2, 2023

Completed
29 days until next milestone

Study Start

First participant enrolled

July 1, 2023

Completed
7 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

February 1, 2024

Completed
6 months until next milestone

Study Completion

Last participant's last visit for all outcomes

August 1, 2024

Completed
Last Updated

June 2, 2023

Status Verified

December 1, 2022

Enrollment Period

7 months

First QC Date

May 24, 2023

Last Update Submit

May 24, 2023

Conditions

Outcome Measures

Primary Outcomes (1)

  • Arterial blood gas as an early screening tool for predicting lung injury in blunt chest trauma

    evaluate the diagnostic accuracy of ABG as a screening tool for identifying and early diagnosis lung injury in adult in blunt chest trauma

    5 minutes after arrival to emergency

Interventions

ABGOTHER

ABG

Eligibility Criteria

Age6 Months+
Sexall
Healthy VolunteersNo
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)
Sampling MethodProbability Sample
Study Population

blunt chest trauma

You may qualify if:

  • \- all patient with polytrauma or blunt trauma to chest and thoraco-abdominal area from both genders are included in the study

You may not qualify if:

  • shocked patients whom were intubated ,patients that had pulmonary disease or heart diseases ,penetrating chest injury ,pregnant female ,patients who do not want to participate in the study

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Central Study Contacts

asmaa ali mohamed, resident

CONTACT

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Assistant lecturer

Study Record Dates

First Submitted

May 24, 2023

First Posted

June 2, 2023

Study Start

July 1, 2023

Primary Completion

February 1, 2024

Study Completion

August 1, 2024

Last Updated

June 2, 2023

Record last verified: 2022-12